明胶
纳米纤维
姜黄素
体内
药物输送
MTT法
静电纺丝
体外
材料科学
细胞毒性
壳聚糖
达皮
化学
生物医学工程
分子生物学
纳米技术
细胞凋亡
医学
生物化学
生物
聚合物
复合材料
生物技术
作者
Bin Jiang,Zhangkai Yang,Hangyu Shi,Abduladheem Turki Jalil,Marwan Mahmood Saleh,Weiyang Mi
标识
DOI:10.1016/j.jddst.2022.104105
摘要
Currently, localized drug delivery vehicles based on implantable electrospun nanofibrous scaffolds have attracted enormous interest in eradicating cancer cells and regenerating the tissue defects after tumor removal. In the present investigation, zeolite Y nanoparticles (nZY) were exploited to load Curcumin (Curc) as a potent natural anticancer agent. Then the synthesized Curc@nZY were integrated into a hybrid of PCL-gelatin electrospun nanofibers (Curc@nZY-PG NFs). XRD, FTIR, FE-SEM, TEM, and BET were exploited to characterize the physicochemical and morphological characteristics of the prepared nanoparticles and NFs. Apart from in vitro drug release testing, MTT assay, scratch assay, DAPI staining, and qPCR were applied to assess the in vitro anticancer efficiency of Curc@nZY-PG NFs against U87-MG glioblastoma cells after three days of incubation time. Based on the findings, it was found that the bead-free, randomly oriented electrospun PG NFs were loaded successfully with Curc@nZY. Also, applying nZY to load Curc into the PG NFs led to a steadier drug release over a relatively long period compared to Curc-PG NFs so that 33.5% and 47% of Curc were liberated from Curc@nZY-PG NFs within 72 h and 14 days, respectively. Besides, the cells exposed to the Curc@nZY-PG NFs exhibited superior cytotoxicity, anti-cell migratory activity, and pro-apoptotic effect against the glioblastoma cells. Therefore, it can be speculated that the development of Curc@nZY-PG composite electrospun mats might act as a highly promising and safe localized drug delivery approach for potential postsurgical glioblastoma treatment.
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